C. R. Bard, Inc.

QA Technician

2 weeks ago(1/2/2018 4:19 PM)
Industry / Category
Manufacturing
Job ID
2017-10852
Career Level
entry level
Division
Carol Stream, IL/BBI
Relocation
No
US-IL-Carol Stream

Overview

Bard Brachytherapy Inc. is in Carol Stream, Illinois, approximately 25 miles from Chicago O’Hare International Airport. For over 100 years, C. R. Bard, Inc. has been Advancing the Delivery of Healthcare by creating innovative products and services that meet the needs of healthcare providers and patients. Today, Bard is a leader in products that focus on Disease State Management in three key areas: Vascular, Urology, and Oncology. To complement these areas, Bard has a complete line of advanced Surgical Specialty Products and Services.

Summary of Position with General Responsibilities

The QA Technician works in the Quality Assurance department and performs general quality control quality assurance testing and review activities in accordance with current Good Manufacturing Practices (cGMP), company policy and safety regulations.

Essential Job Functions

  • Product and raw material quarantine, inspection, and release;
  • Review and release of processed customer orders and records;
  • Review and release of production manufacturing records;
  • Ensures compliance to departmental procedures;
  • Understand and follow product drawings;
  • Lab cleaning;
  • General data / documentation review and archive

 

Other duties may be assigned, including but not limited to:

  • General quality control / quality assurance;
  • Environmental sampling activities

Basic Qualifications

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed are representative of the knowledge, skill and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. •Strong organizational skills; •Proficiency in math; •Strong attention to detail; •Ability to work independently; •Excellent oral and written communication skills in English. •Ability to read and interpret data to reach a sound decision; read, interpret, and relay department requirements to other areas or staff. •Ability to work 2nd shift and overtime.

Additional Desirable Qualifications Skills and Knowledge

  • Previous work in a Medical Device/FDA regulated environment is preferred
  • Knowledge of FDA GMP, ISO 9001, or ISO 13485 quality system requirements is a plus

Education and/or Experience

Required

  • High school diploma, or equivalent
  • Basic computer skills
  • Ability to work 2nd shift (2pm or later start) and overtime

 Preferred

  • College degree
  • Experience in a FDA regulated industry and/or QA environment
  • Proficient in the use of a PC with an intermediate level of keyboarding skills
  • Proficient in the use of JDEdwards ERP System

Salary starting at $16.00/hour (commensurate with experience)

Physical Demands

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.  Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

 

Required to sit, talk, hear, stand, bend, reach with hands, lift or move up to 25 lbs. (archive record boxes).  Vision requirements include ability to see and interact with a computer.

Work Environment

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job.  Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

 

This position works in a normal office environment.  The noise level in the work environment is quiet to moderate. May include manufacturing or lab environment and certain work areas contain radioactive or hazardous chemicals.

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